A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3174387



Internal ID22332783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93600172..93600652hg38UCSC Ensembl
chr5:92935878..92936358hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14436430
SamplesHG00514
Known GenesMIR548AO
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3174387
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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